Ablation device

ABSTRACT

An ablation device comprises a balloon having an open proximal end and a closed distal end. A cylindrical tube extends into the balloon through the proximal end. An end support member is positioned at the distal end of the balloon. The end support member comprises a cylindrical portion facing the proximal end of the balloon. The cylindrical portion is received within a bore at the distal end of the tube. A seal is formed between the proximal end of the balloon and the cylindrical tube.

CROSS-REFERENCE TO RELATED APPLICATION

This application is a continuation-in-part of U.S. utility application Ser. No. 13/152,825 filed Jun. 3, 2011, and this application claims the benefit of U.S. provisional application Ser. No. 61/424,262 filed Dec. 17, 2010. Each of the above-referenced applications are hereby incorporated herein by reference in their entirety.

BACKGROUND OF THE INVENTION

Pelvic conditions include diseases of the uterus, such as uterine fibroids and menorrhagia. Uterine fibroids are non-cancerous tumors of the uterus that typically appear on the endometrium layer (i.e., uterine wall) of the uterus. Menorrhagia is a medical condition involving excessive and difficult to control bleeding of the endometrial layer of the uterus. These conditions have been treated through hysterectomy. However, alternative, less radical approaches are also being used.

One alternative to a hysterectomy is endometrial ablation, which induces necrosis of the endometrial layer and a portion of the myometrial layer. These treatments can include freezing and heating the endometrial layer, or cauterizing the endometrial layer using a laser.

SUMMARY

Embodiments of the invention are directed to an ablation device for use with the laser ablation system to perform an ablation treatment of an interior cavity of a patient. In one embodiment, the device includes a balloon having an open proximal end and a closed distal end. A cylindrical tube extends into the balloon through the proximal end. An end support member is positioned at the distal end of the balloon. The end support member comprises a cylindrical portion facing the proximal end of the balloon. The cylindrical portion is received within a bore at the distal end of the tube. A seal is formed between the proximal end of the balloon and the cylindrical tube.

Another embodiment of the ablation device comprises a balloon having a proximal end, a closed distal end and a central axis. A cylindrical tube extends into the balloon through the proximal end. A central support member is located within the balloon and has a central opening through which the tube extends. The central support member extends radially from the tube. A seal is formed between the proximal end of the balloon and the cylindrical tube.

Another embodiment of the ablation device comprises a balloon having an open proximal end and an open distal end. A cylindrical tube extends through the proximal end of the balloon. A first seal is formed between the open proximal end of the balloon and the cylindrical tube. A laser fiber extends through the cylindrical tube. The laser fiber includes a light dispenser. The light dispenser is configured to deliver laser light through the cylindrical tube and the balloon. A portion of the balloon surrounding the open distal end is between the laser fiber and a distal end of the tube.

Other features and benefits that characterize embodiments of the present invention will be apparent upon reviewing the following detailed description and the associated drawings.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a simplified diagram of a laser tissue ablation system formed in accordance with embodiments of the invention.

FIGS. 2 and 3 are simplified cross-sectional views illustrating the attachment of a distal end of a shaft to a balloon, in accordance with exemplary embodiments.

FIG. 4 is an end view of an end support member in accordance with embodiments of the invention.

FIGS. 5 and 6 are simplified diagrams of an inflated balloon in accordance with embodiments of the invention.

FIG. 7 is a side cross-sectional view of a distal end of the ablation device in accordance with embodiments of the invention.

FIG. 8 is a cross-sectional view depicting pelvic anatomy of a female patient and a distal end of the ablation device formed in accordance with embodiments of the invention.

FIG. 9 is an isometric view of a balloon in accordance with embodiments of the invention.

FIGS. 10 and 11 are side cross-sectional views of a distal end of an ablation device illustrating fluid or gas flow in accordance with embodiments of the invention.

FIG. 12 is a cross-sectional view of the distal end of the ablation device in accordance with embodiments of the invention.

FIGS. 13 and 14 are side views of light dispensers in accordance with embodiments of the invention.

FIGS. 15 and 16 are side views of the distal end of the ablation device illustrating laser fiber positioning components in accordance with embodiments of the invention.

FIG. 17 is a simplified diagram of the ablation device including a handheld unit in accordance with embodiments of the invention.

FIGS. 18-20 respectively show isometric assembled, isometric exploded and magnified isometric views of the applicator with a handheld unit formed in accordance with exemplary embodiments of the invention.

DETAILED DESCRIPTION OF ILLUSTRATIVE EMBODIMENTS

Embodiments of the present invention are directed to a laser tissue ablation device designed to perform tissue ablation and/or other laser treatments on a patient. While particular embodiments of the invention will be described as useful in treating menorrhagia through endometrial ablation of the uterine wall of a patient, those skilled in the art understand that the system of a present invention may be adapted to perform ablation treatments of other tissue of a patient, such as that of the anal cavity, the bladder, the vagina, the esophagus, the trachea, the urethra, the ureter, the prostate gland, the kidney, intestinal growths or abnormal tissues of the intestine (e.g., hemorrhoids, polyps, etc.) and cancerous tissues.

FIG. 1 is a simplified diagram of a laser tissue ablation system 100 formed in accordance with embodiments of the invention. One embodiment of the system 100 includes an ablation device 102 that is formed in accordance with one or more embodiments described below.

One embodiment of the device 102 comprises a shaft or cylindrical tube 104 having a proximal end 106 and a distal end 108. One embodiment of the shaft 104 is formed of a rigid and substantially transparent material, such as, for example, acrylic, PET, silicone, polyurethane, polycarbonate, glass or other suitable material. In one embodiment, the device 102 includes a balloon 110 that is attached to the shaft 104 proximate the distal end 108. In one embodiment, the balloon 110 comprises a proximal end 112 and a distal end 114. In one embodiment, the proximal end 112 is attached to the shaft 104 by a sleeve 116 that is formed, for example out of Teflon®, which seals an opening of the balloon 110 to the shaft 104.

In one embodiment, the distal end 108 of the shaft 104 is attached to the distal end 114 of the balloon 110. In one embodiment, the shaft 104 has a longitudinal axis 117. In one embodiment, the distal end 108 of the shaft 104 is secured to the distal end 114 of the balloon 110 along longitudinal axis 117. In one embodiment, the longitudinal axis 117 is aligned with a central axis 118 of the balloon 110. In one embodiment, the balloon is symmetric about the longitudinal or central axis 117 when inflated.

The attachment of the balloon 110 to the shaft 104 can be accomplished in many different ways. FIG. 2 is a cross-sectional view illustrating an exemplary means of attaching the shaft 104 to the balloon 110 using a cap 119. The cap 119 comprises a cylindrical portion 120 that is received within a bore 122 of the shaft 104. The distal end 114 of the balloon 110 is captured between the surfaces of the cylindrical portion 120 of the cap 119 and the shaft 104. In one embodiment, frictional resistance prevents the cap 119 from becoming dislodged from the bore 122 of the shaft 104. A biocompatible adhesive may also be used to secure the cap 119 to the distal end 108 of the shaft 104. Other techniques may also be used to secure the balloon 110 to the distal end 108 of the shaft 104.

FIG. 3 is a cross-sectional view illustrating the attachment of the shaft or cylindrical tube 104 to the distal end of the balloon 110 in accordance with other embodiments of the invention. In one embodiment, the cylindrical tube 104 extends into the balloon 110 through the proximal end 112 as shown in FIG. 1. In one embodiment, an end support member 123 is positioned at the distal end 114 of the balloon 110. In one embodiment, the end support member 123 is attached to an interior side or wall 124 of the balloon 110. In one embodiment, the end support member 123 comprises a cylindrical portion 125 facing the proximal end 112 of the balloon 110. In one embodiment, the cylindrical portion 125 is received within the bore 122 at the distal end 108 of the tube 104. In one embodiment, the cylindrical portion 125 is slightly compressed within the bore 122 to facilitate attachment of the tube 104 to the member 123.

FIG. 4 is an end view of the end support member 123 in accordance with embodiments of the invention. In one embodiment, the support member 123 comprises an annular groove 126 surrounding the cylindrical portion 125, as shown in FIG. 4. In one embodiment, the distal end 108 of the tube 104 is received within the annular groove 126, as shown in FIG. 3.

In one embodiment, the end support member 123 is coaxial to the central axis 118 of the balloon. In one embodiment, the annular groove 126 is coaxial to the central axis 118. As a result, the insertion of the distal end 108 of the cylindrical tube 104 in the annular groove 126 positions the distal end 108 in a generally coaxial relationship to the central axis 118, as shown in FIG. 3.

The balloon 110 has a deflated state 127 (phantom line) and an inflated state 128 (solid line), as shown in FIG. 1. The deflated state 127 of the balloon 110 is preferably sufficiently compact to allow the distal end 108 of the shaft 104 and the attached balloon 110 to be inserted into the desired cavity of the patient, such as the uterus or vagina, to locate the balloon 110 proximate the tissue targeted for treatment. In one embodiment, the deflated state of the balloon 110 is approximately 4-6 mm or less in diameter measured radially from the central axis 118 of the balloon 110. When in the inflated state 128, the balloon 110 substantially conforms to the cavity in which it is placed.

In one embodiment, the balloon 110 is be formed of a suitable biocompatible material. In one embodiment, the balloon 110 is formed of a distensible material, such as silicone, PET, polyurethane, rubber or other suitable material. The distensible material can stretch responsive to inflating the balloon 110 from the deflated state 127 to the inflated state 128, as shown in FIG. 1, due to an increase in the pressure of the interior 124 of the balloon 110. The distensible material allows the balloon 110 to further conform to the cavity of the patient in which it is placed in response to pressure exerted on the balloon 110 from the walls of the cavity.

In accordance with another embodiment, the balloon 110 is formed of minimally distensible material, such as polyurethane, or other suitable material.

In one embodiment, the balloon 110 includes an Inhibizone coating, such as that described in U.S. Pat. No. 5,756,145, which is incorporated herein by reference in its entirety.

FIGS. 5 and 6 are simplified diagram of the balloon 110 in the inflated state 128, in accordance with embodiments of the invention. In one embodiment, the inflated state 128 of the balloon 110 has a cylindrical shape with a rounded distal end 114, as illustrated in FIGS. 1 and 5.

In accordance with another embodiment, the inflated state 128 of the balloon 110 has a predefined non-cylindrical or spherical shape that conforms to the interior cavity of the patient where the tissue targeted for ablation is located. One exemplary embodiment is illustrated in the simplified side view of FIG. 6, in which the inflated state 128 of the balloon 110 is shaped to conform to the uterus of a patient. The balloon 110 can take on other cavity-conforming shapes, such as the shape of the vagina, the anal cavity, the esophagus, the trachea, the bladder, or other cavity within the body.

When the balloon 110 is formed of substantially non-distensible material, the predefined inflated shape 126 of the balloon 110 will drive the tissue of the cavity into conformity with the balloon 110. When the balloon 110 is formed distensible material, the inflated state 128 of the balloon will generally conform to the cavity of the patient. As a result, the balloon 110 may only minimally deflect the walls of the cavity when the balloon is inflated. Further, the balloon 110 will also deform in response to engagement with the walls of the cavity.

In one embodiment, the pre-defined shape of the inflated state 128 of the balloon prevents the balloon from applying significant pressures to the walls of the cavity of the patient. In one embodiment, the balloon 110 applies less than 10 psi to the walls of the cavity of the patient in which it is inflated. Thus, the balloon 110 having a pre-defined inflated shape can significantly reduce the pressure on the walls of the cavity of the patient in which the balloon 110 is inflated. This can reduce patient intraoperative and post operative pain.

In one embodiment, the ablation device 102 includes a central support member 129 within the balloon 110 that serves the purpose of maintaining a desired displacement of the balloon 110 from the central axis 118, as shown in the side cross-sectional view of a distal end of the ablation device 102 provided in FIG. 7. In one embodiment, the central support member 129 includes a central opening 130 through which the shaft or cylindrical tube 104 extends. In one embodiment, the central opening 130 is coaxial to the central axis 118. The central support member 129 extends from the tube 104 radially from the central axis 118 of the balloon 110 and ensures a radial displacement of the balloon 110 from the tube 104. The support member 129 can include holes 131 to allow for the flow of fluid or gas through the member 129. In one embodiment, the central support member 129 is located along the central axis 118 intermediate the proximal end 112 and the distal end 114 of the balloon. In one embodiment, the central support member 129 is positioned along central axis 118 closer to the distal end 114 of the balloon 110 than the proximal end 112, as shown in FIG. 7. While only one central support member 129 is depicted, it is understood that other central support members can be added at different locations along the central axis 118 to provide the desired minimal displacement of the balloon 110 from the central axis 118. Additionally, while the balloon 110 is illustrated as being substantially cylindrical, support members 129 having different sizes and shapes may be used to direct the balloon 110 into a non-uniform shape.

FIG. 8 is a cross-sectional view of a female patient depicting the vagina 132, the cervix 134 and the uterus 136. The distal end 108 of the shaft 104 and a balloon 110 are inserted through the cervix 134 and into the uterus 136 when the balloon 110 is in the deflated state 127. The balloon 110 is then expanded to the inflated state 128 (shown), in which the balloon 110 substantially conforms to the shape of the uterine wall 138. The balloon 110 preferably engages the uterine wall 138 while applying minimal pressure. In one embodiment, the balloon 110 applies less than 10 psi to the uterine wall 138 when in the inflated state 128.

In one embodiment, the balloon 110 includes markings 139, as shown in FIG. 9. The markings 139 can be viewed from within the interior 124 to determine whether the balloon 110 is properly inflated and/or positioned within the cavity of the patient. In one embodiment, the markings 139 comprise one or more visible lines extending longitudinally (i.e., lines 139A), and/or circumferentially (i.e., lines 139B) around the balloon 110. In one embodiment, the markings 139 comprise a grid pattern.

In one embodiment, the balloon 110 seals the distal end 108 of the shaft 104. A seal 142, such as an o-ring, or other suitable seal, seals the proximal end 106 of the shaft 104.

In one embodiment, the balloon 110 may be inflated with fluid or gas, such as a saline solution. In one embodiment, the shaft 104 includes a port 140, as shown in FIG. 1, through which the fluid or gas may be received. In one embodiment, the system 100 comprises a pump 144 that drives a fluid or gas from a supply 146 through the port 140 and into the interior 124 of the balloon 110 to drive the balloon 110 to its inflated state 128. The pump 144 can take on many different forms. In one embodiment, the supply 146 is in the form of a pressurized gas, in which case, the pump 144 may represent a valve that controls the flow of the gas from the supply 146. In accordance with another embodiment, the pump 144 drives a fluid from the supply 146 through the port 140 and into the interior 124 of the balloon 110 to inflate the balloon 110. Embodiments of the pump 144 include a syringe, a diaphragm pump, gear pump, or other suitable pump.

In one embodiment, gas or fluid enters the shaft 104 through the port 140, shown in FIG. 1. In one embodiment, the shaft 104 includes a fluid path 149 that fluidically couples the port 140 to openings 148 in the shaft 104 to the interior 124 of the balloon 110, as shown in FIG. 7. The gas or fluid entering the port 140 flows through the fluid path 149, through the openings 148 and into the interior 124 of the balloon 110 as shown in FIGS. 1 and 7. In accordance with one embodiment, the fluid or gas within the interior cavity 124 of the balloon 110 may be discharged back through the openings 148 of the shaft 104 and out the port 140. Alternatively, as shown in FIG. 10, the fluid or gas within the interior cavity 124 of the balloon 110 may be discharged through one or more openings 150 to a fluid path 152 that is connected to a dedicated drain port 154 (FIG. 1).

In accordance with one embodiment, the balloon 110 comprises an interior balloon 110A and an exterior balloon 110B, as shown in the simplified side-cross sectional view of FIG. 11. In accordance with one embodiment, either the interior balloon 110A or the exterior balloon 110B is formed of a non-distensible material, while the other balloon 110A or 110B is formed of a distensible material. In one embodiment, the interior balloon 110A is formed of a substantially non-distensible or minimally distensible material and has a predefined shaped in accordance with embodiments described above. In accordance with one embodiment, a biocompatible lubricant is located between the interior balloon 110A and the exterior balloon 110B.

In accordance with one embodiment, the fluid or gas driven through the port 140 is fed between the interior balloon 110A and the exterior balloon 110B, as represented by the arrows in FIG. 11. In one embodiment, the fluid is discharged through the fluid path 152 and out the drain port 154. The flow of fluid between the balloons 110A and 110B can be used to control the temperature of the tissue that is in contact with the balloon 110B.

One embodiment of the system 100 includes a conventional laser source 160 that can be attached to a waveguide 162, such as an optical fiber (hereinafter “laser fiber”), that can be received within the shaft 104. The laser source 160 can be a conventional laser generating system. In accordance with one embodiment, the laser source 160 is configured to generate laser light or a laser 164 having a desired wavelength for performing surgical procedures, such as tissue ablation.

In one embodiment, the laser source 160 is configured to produce an Nd:YAG laser operating at approximately 532 nanometers or 1064 nanometer wavelengths. The laser source 160 may be a solid state laser based on a potassium-titanyl-phosphate (KTP) crystal, a lithium triborate (LBO) laser, a beta barium borate (BBO), a holmium laser and a thulium laser, or other type of laser source used to perform tissue ablation or other laser treatment. Exemplary laser sources 160 are described in U.S. Pat. No. 6,986,764 (Davenport), which is incorporated herein by reference in its entirety.

The laser 164 generated by the laser source 160 travels through the laser fiber 162 and is discharged through a light dispenser 166 at a distal end 168. In one embodiment, the dispensed laser light 164 is transmitted through the shaft 104 and the balloon 110 and onto the targeted tissue of the patient, such as the uterine wall 138 shown in FIG. 8.

In one embodiment, the distal end 168 of the laser fiber 162 is supported in fixed relation to the distal end 114 of the balloon 110. In one embodiment, the end support member 123 includes a recess 169 that is formed within the cylindrical portion 124, as shown in FIG. 3. In one embodiment, the recess 169 is coaxial to the central axis 118 of the balloon and supports the laser fiber 162 in alignment with the central axis 118, as shown in FIG. 3. In one embodiment, the laser fiber 162 includes an extension portion 170 at the distal end 168 that is received in the recess 169. The extension portion 170 is located distally from the dispenser 166, as shown in FIG. 3.

FIG. 12 is a cross-sectional view of the distal end of the device 102 in accordance with embodiments of the invention. One embodiment of the balloon 110 includes the opening at the proximal end 112 (FIG. 1) and an opening 171 at the distal end 114, as shown in FIG. 12. In one embodiment, the tube 104 extends through the opening at the proximal end 112 of the balloon 110 (FIG. 1) and into the interior 124 of the balloon 110. The proximal end 112 of the balloon 110 is sealed against the tube 104, as discussed above. In one embodiment, a seal is formed between the opening 171 of the distal end 114 of the balloon 110 and the extension portion 170 of the laser fiber 162. In one embodiment, a portion 172 of the distal end of the balloon 110 surrounding the opening 171 is positioned between the extension portion 170 of the laser fiber 162 and the distal end 108 of the tube 104. In one embodiment, the extension portion 170 is glued to the portion 172 of the balloon 110 using a suitable biocompatible adhesive.

Embodiments of the light dispenser 166 are configured to discharge the laser light 164 in a desired manner, such as along the axial and/or radial directions of the laser fiber 162, to one side of the laser fiber 162, in a diffuse pattern around the dispenser 166, and/or other desired manner. Exemplary light dispensers 166, such as side-fire optical caps, are disclosed in U.S. Pat. Nos. 5,428,699 (Pon), U.S. Pat. No. 5,269,777 (Doiron et al.), U.S. Pat. No. 5,530,780 (Ohsawa), and U.S. Pat. No. 5,807,390 (Fuller et al.).

In one embodiment, the light dispenser 166 comprises an etched section 173 of the laser fiber 162, as shown in FIG. 13, to dispense the laser light 164 in a diffuse pattern. In one embodiment, portions of the etched section 173 are tapered to direct the diffused laser light in a desired manner, such as axially. The etching can be made using an appropriate laser, such as a CO₂ laser, to roughen the exterior surface of the laser fiber 162. In one embodiment, a cap 174 encloses the dispenser 166, as shown in FIG. 13.

If the laser light 164 is output from the dispenser 166 in an even dispersion pattern, the targeted tissue located farther away will receive less laser light energy than the targeted tissue located closer to the dispenser 166. In one embodiment, the etching pattern of the section 173 is customized to include portions that transmit more light energy than other portions to customize the laser energy dispersion pattern output from the dispenser 166. That is, the etched section 173 may comprise different patterns in different portions of the section 173 to provide different levels of laser light transmission through the different portions of the section 173. This allows the targeted tissue to receive similar intensity levels of the dispensed laser light 164 even though the targeted tissue is not located a uniform distance from the dispenser 166.

In accordance with one embodiment, light transmission through the balloon 110 is non-uniform. In one embodiment, light transmission through the balloon varies along the central axis 118 of the balloon 110. That is, portions of the balloon 110 at different locations along the axis 118 (e.g., portions in a plane that is perpendicular to the axis 118) have a degree of laser transparency that is different from other portions of the balloon along the axis 118. This allows for the control of the transmission of the laser light 164 through the balloon 110 and, therefore, the amount of laser energy that is delivered to the targeted tissue.

In one embodiment, the material forming the balloon provides a predefined pattern of laser transparency variation along the axis 118, such as, for example, by varying a thickness of the balloon 110. In one embodiment, printing or a coating of material on of the balloon 110, such as on the interior wall 124 (FIG. 1), defines the desired pattern of laser transparency though the balloon 110. In one embodiment, the printing or coating defines the pattern of laser transparency by applying the printing or coating to select portions of the balloon 110, applying the printing or coating in a varying pattern on the balloon 110, and/or applying the printing or coating in a varying thickness on the balloon 110. Embodiments of the coating may comprise titanium dioxide (TiO₂), Tampapur Ink, and/or parylene. In one embodiment, the coated or printed material is reflective.

FIG. 14 illustrates a simplified diagram of a light dispenser 166 in accordance with another embodiment of the invention. In accordance with this embodiment, the light dispenser 166 comprises a plurality of glass beads 175 within the balloon 110. The laser light is discharged through the distal end 168 of the laser fiber 162 and interacts with the glass beads 175 to disperse the laser light 164 around the surface of the balloon 110.

In one embodiment, the distal end 108 of the shaft 104 is configured to transmit the laser light 164 discharged through the dispenser 166 of the laser fiber 162 at varying degrees of efficiency. That is, sections of the shaft 104 are configured to be more transparent to the laser light 164 than other sections of the shaft 104. This pattern of laser transparency of the shaft may be formed in various ways. In one embodiment, the interior or exterior wall of the shaft 104 is coated as described above with regard to the balloon 110. Alternatively, the pattern may be formed on the shaft 104 by etching the pattern on the shaft 104, applying a particulate to the shaft 104 that blocks the laser light 164, tinting the shaft 104, or other suitable technique for creating the desired pattern of laser transparency through the shaft 104. As discussed above with regard to the dispenser 166 illustrated in FIG. 13, the control of the transmission of the laser light 164 through the shaft 104 provides control over the amount of laser energy that is delivered to the targeted tissue.

One embodiment of the system 100 includes one or more laser fiber positioning components 180 represented schematically in FIG. 1. In one embodiment, the positioning components 180 are configured to move the laser fiber 162 axially along the longitudinal axis of the laser fiber, as indicated by arrow 176 in FIG. 1, relative to the shaft 104 and/or the balloon 110. This axial movement of the distal end 168 laser fiber 162 causes the laser fiber 162 to generally move along the longitudinal axis 117 of the shaft 104 and along the central axis 118 of the balloon 110 relative to the balloon 110 and the shaft 104. In accordance with one embodiment, the distal end 168 of the laser fiber 162 may be moved axially by the one or more components 180 to withdraw the distal end 168 and the dispenser 166 of the laser fiber 162 from within the interior 124 of the balloon 110. The components 180 may also move the distal end 168 and the dispenser 166 of the laser fiber 162 into the interior 124 of the balloon 110. Thus, the dispenser 166 of the laser fiber 162 may be positioned in the desired location relative to the balloon 110 and the shaft 104 using the one or more laser fiber positioning components 180.

In accordance with another embodiment, the laser fiber positioning components 180 are configured to rotate the laser fiber 162 about its longitudinal axis and, thus, rotate (i.e., move angularly) the dispenser 166 about the longitudinal axis. This may be useful when the dispenser 166 is configured to output the laser light 164 radially out a side of the dispenser 166 over a range of less than 360 degrees. With such a configuration, the dispenser 166 can be made to output the laser light 164 to the tissue surrounding the dispenser 166 by rotating the dispenser 360 degrees using the positioning components 180.

In accordance with one embodiment, the one or more positioning components 180 are configured to move the distal end 168 of the laser fiber 162 in an arc relative to the balloon 110. FIGS. 15 and 16 illustrate exemplary components 180 for moving the distal end of the laser fiber 162 in an arc. In one embodiment, the components 180 comprise at least two balloons 182 and 184 that may be inflated and deflated through the pumping of a gas or fluid through suitable conduit (not shown) coupled to the balloons 182 and 184. In one embodiment, the distal end 168 of the laser fiber 162 is not covered by the shaft 104. Movement of the distal end 168 of the laser fiber 162 along an arc in the direction indicated by arrow 186 is accomplished by deflating the balloon 184 and inflating the balloon 182, as shown in FIG. 15. Likewise, the distal end 168 of the laser fiber 162 may be moved in an arc in the direction indicated by arrow 188 by deflating the balloon 182 and inflating the balloon 184, as shown in FIG. 16. Additional balloons may be used in a similar manner to displace the distal end 168 of the laser fiber 162 along an arc in the desired direction.

One embodiment of the system 100 includes a viewing system 200 that is configured to provide the physician with a view from the interior 124 of the balloon 110. One embodiment of the viewing system 200 comprises a viewing fiber 202 that is received within the shaft 104, as shown in FIG. 1. In one embodiment, the distal end 204 comprises an imaging component 206, such as a charge coupled device (CCD) that is configured to image the interior 124 of the balloon 110 through the shaft 104. The imaging component 206 may be a conventional device that includes the necessary electronics to deliver the image data down the viewing fiber 202 to a suitable viewing console 208 through one or more wires (not shown). A capsule or other protective means can protect the imaging component 206 from the environment within the interior 124 of the balloon 110.

In one embodiment, the viewing system 200 includes one or more viewing fiber positioning components 210 that are configured to adjust the position and/or orientation of the imagining component 206 to image the desired portion of the balloon 110 or the targeted tissue of the patient. In one embodiment, the positioning components 210 are configured to move the viewing fiber 202 axially along the longitudinal axis of the viewing fiber, as indicated by arrow 211 in FIG. 1. relative to the shaft 104 and/or the balloon 110. Accordingly, the distal end 204 of the viewing fiber 202 may be moved axially by the one or more components 210 to withdraw the imaging component 206 from within the interior 124 of the balloon 110. The imagining component 206 can be moved from this withdrawn position into the interior 124 of the balloon 110 and positioned in a desired location relative to the balloon 110 and the shaft 104. In accordance with another embodiment, the viewing fiber positioning components 210 are configured to rotate the viewing fiber 202 about its longitudinal axis and, thus, rotate the imagining component 206 about the longitudinal axis of the viewing fiber 202. This allows the imaging component 206 to image a full 360° around the longitudinal axis of the viewing fiber 202.

Exemplary positioning components for the laser fiber 162 and the components 210 for the viewing fiber 202 include components that facilitate the hand feeding of the fibers 162 and 202, and components that drive the feeding of the laser fiber 162 and the viewing fiber 202, such as rollers that are rotated by hand or driven by a motor, or other suitable mechanism for feeding the laser fiber 162 and the viewing fiber 202 in their axial directions. In one embodiment, the components 180 and 210 are configured to rotate the laser fiber 162 and the viewing fiber 202, respectively, and include components that facilitate the rotation of the fibers by hand, mechanisms that are driven by hand or by a motor that engage the fibers and rotate the fibers about their longitudinal axis, or other components that can be used to rotate the fibers.

Another embodiment of the system 100 includes one or more sensors 212 (FIG. 1) that are configured to sense a parameter of the system 100 and/or the patient. One embodiment of the sensors includes a temperature sensor, such as a thermal couple, that is configured to sense the temperature of the balloon 110 and/or the tissue of the patient. In accordance with one embodiment, when the balloon 110 comprises and internal balloon 110A and an external balloon 110B (FIG. 11), the temperature sensor is located between the balloons 110A and 110B. In accordance with another embodiment, the sensors 212 include a pressure sensor configured to detect a pressure of the interior 124 of the balloon 110. In one embodiment, the system 100 includes a sensor in the form of a flow meter 213 (FIG. 1) that is configured to detect the flow rate of fluid driven by the pump 144. Signals from the one or more sensors 212 are fed via wires or other conventional means to a controller 214 that can use the information received from the sensors 212 to control components of the system 100, such as the pump 144.

One embodiment of the device 102 comprises a handheld unit 220, an exemplary embodiment of which is illustrated in FIG. 17. The handheld unit 220 is generally configured to support components of the device 102 described above. In one embodiment, the unit 220 is configured to support the proximal end 106 of the shaft 104. In one embodiment, the unit 220 is configured to support the laser fiber 162. In accordance with other embodiments, the handheld unit 220 is configured to support the viewing fiber 202, the one or more laser fiber positioning components 180 and/or the one or more viewing fiber positioning components 210 described above. In accordance with another embodiment, the handheld unit 220 is configured to receive tubing 250 used to pump fluid or gas through the shaft 104 and into the balloon 110.

In one embodiment, the handheld unit 220 allows the laser fiber 162 to pass through the body of the unit 220 for attachment to the laser system 160. Similarly, the handheld unit 220 allows for the viewing fiber 202 to pass through the body of the unit 220 for coupling to the viewing system 208.

In one embodiment, the handheld unit 220 supports a laser actuator 222 that is configured to trigger the laser system 160 to deliver laser energy down the laser fiber 162 to the distal end 168. Embodiments of the laser actuator 222 include a button, a finger trigger, or other suitable mechanism. One embodiment of the laser actuator 222 that is not supported by the handheld unit 220 is a foot-activated switch.

FIGS. 18-20 respectively show isometric assembled, isometric exploded and magnified isometric views of the device 102 with a handheld unit 220 formed in accordance with exemplary embodiments of the invention. In one embodiment, the handheld unit 220 comprises a pistol grip 230 and a support member 232 that extends transversely to the pistol grip 230. In one embodiment, the support 232 comprises a hinged cover 234 having a closed position (FIG. 18) and an opened position (FIG. 19). A bore 236 is formed in the support 232 and/or the cover 234 and is sized to receive the shaft 104, as shown in FIG. 20. In one embodiment, the shaft 104 is securely held within the bore 236 when the cover 234 is in the closed position such that inadvertent movement of the shaft 104 in the longitudinal direction during normal handling of the device 102 is prevented. In one embodiment, the support 232 and/or the cover 234 includes a shoulder portion 238 at a proximal end 240 of the bore 236 that prevents the shaft 104 from sliding toward the rear 242 of the support 232 along the longitudinal axis.

In one embodiment, the support 232 and/or the cover 234 comprise a channel 244 that is configured to receive the laser fiber 162, as best shown in FIG. 16. The channel 244 extends to the shoulder portion 238 where it receives the laser fiber 162 where it exits the shaft 104. The channel 244 extends from the shoulder 238 out the rear end of the support 232 where it can be coupled to the laser system 160 in a conventional manner.

Another embodiment of the handheld unit 220 comprises a channel 246 formed in the support 232 and/or the cover 234, as best shown in FIG. 20. The channel 246 extends from the shoulder portion 238 out the rear end 242 of the support 232. The channel 246 is configured to receive the viewing fiber 220 as it exits the proximal end 106 of the shaft 104 and allows the viewing fiber 202 to extend out the rear end 242 of the support member 232 where it can be connected to the viewing system 208.

In one embodiment, the handheld unit 220 includes a channel 248 configured to receive conduit 250 that is coupled to the fluid input port 140, as shown in FIG. 20. In one embodiment, the channel 248 extends through the support 232 and the pistol grip 230. The exposed end of the conduit 250 may be coupled to the flow meter 213 or pump 144 using conventional means.

As discussed above, one embodiment of the handheld unit 220 includes the one or more laser fiber positioning components 180. In one embodiment, the laser fiber positioning components 180 comprise a thumb wheel 252 that is coupled to a roller 252 through a gear, axle, or other suitable arrangement, as shown in FIG. 19. The roller 252 engages the laser fiber 162 through a slot 256 in the support 232, as shown in FIG. 20. One embodiment of the roller 252 comprises an exterior surface that comprises rubber or other suitable material that provides sufficient frictional resistance with the exterior of the laser fiber 162 to grip the laser fiber 162 and inhibit sliding contact between the roller 254 and the laser fiber 162. Rotation of the thumb wheel 252 rotates the roller 254, which drives the longitudinal movement of the laser fiber 162 in either the forward or rearward direction relative to the handheld unit 220 and the shaft 104. Thus, one may move the distal end 168 of the laser fiber 162 relative to the balloon 110 to position the distal end 168 as desired.

One embodiment of the one or more viewing fiber positioning components 210 includes a thumb wheel 258 and a roller 260 that operate similarly to the thumb wheel 252 and roller 254 described above to move the viewing fiber 202 in the longitudinal direction relative to the handheld unit 220, the shaft 104 and the balloon 110. The thumb wheel 258 is coupled to the roller 260 through a suitable arrangement, such as a gear. The roller 260 is exposed to engage the viewing fiber 202 through a slot 262 in the support 232. The roller 260 comprises an exterior surface that is formed of a material (e.g., rubber) that generates sufficient frictional resistance with the viewing fiber 202 to inhibit sliding contact between the roller 260 and the viewing fiber 202 as the roller 260 is rotated. Rotation of the thumb wheel 258 causes the roller 260 to rotate, which drives the viewing fiber in the longitudinal direction relative to the handheld unit 220, the shaft 104 and the balloon 110. Thus, the longitudinal position of the distal end 204 of the viewing fiber 202 can be positioned as desired relative to the balloon 110 using the thumb wheel 258.

Another embodiment of the handheld unit 220 comprises one or more viewing fiber positioning components 210 that are configured to rotate the viewing fiber 202 about its longitudinal axis. One embodiment of the components 210 comprise a rotatable member 264, such as a thumb wheel, and a roller 266. The rotatable member 264 is coupled to the roller 266 through an axel, gear, or other suitable arrangement, such that rotation of the member 264 causes the roller 266 to rotate. In one embodiment, the axes of rotation of the member 264 and the roller 266 are parallel to the longitudinal axis of the viewing fiber 202 and the channel 246. The roller 266 engages the viewing fiber 202 through a slot 268. The exterior surface of the roller 266 is formed of a material (e.g., rubber) that produces sufficient frictional resistance with the viewing fiber 202 to inhibit sliding contact with the viewing fiber 202 as the roller 266 rotates. The rotation of the member 264 causes the roller 266 to rotate, which drives the rotation of the viewing fiber 202 about its longitudinal axis. This allows the distal end 204 of the viewing fiber 202 to be rotated as desired within the balloon 110. One embodiment of the one or more laser fiber positioning components 180 includes components that are similar to the rotatable member 264 and the roller 266 that can be used to rotate the laser fiber 162 about its longitudinal axis.

In one embodiment, the handheld unit 220 includes the laser actuator 222 in the form of a trigger 270 that is mounted to the support 232. In one embodiment, actuation of the trigger 270 directs the laser system 160 to transmit laser light through the laser fiber 162 for discharge through the dispenser 166.

In one embodiment, the shaft 104, the balloon 110, the laser fiber 162, the viewing fiber 202, the tubing 250, and/or the port 140 form a disposable group of components. In one embodiment, one or more of these components are provided as a kit in sterilized packaging. In one embodiment, one or more of these components come pre-assembled. For instance, a disposable assembly may comprise the shaft 104, the balloon 110, the laser fiber 162 and the tubing, as shown in FIG. 19, that is ready for installation within the handheld unit 220. One or more of the other components described above, such as the seal 142, may also be included the disposable assembly.

Additional embodiments of the invention include methods of ablating tissue of a patient, or performing another laser treatment, using the system 100. In one embodiment of the method, the system 100 formed in accordance with one or more embodiments described above is provided and the system is prepared for the ablation operation. This may involve the providing of the disposable assembly described above in, for example, sterilized packaging. The disposable assembly is then installed in the handheld unit 202.

In one embodiment, the laser fiber 162 is connected to the laser system 160. In one embodiment, the viewing fiber 202 (if present) is connected to the viewing console 208. In one embodiment, the tubing 250 is fluidically coupled to the pump 144. In one embodiment, connections are made between the one or more sensors 212 and the controller 214.

In one embodiment, a coating, such as an adjuvant, is applied to the exterior surface of the balloon 110, which is placed in contact with the target tissue when the balloon 110 is inflated within the cavity of the patient. The adjuvant is designed to enhance laser tissue ablation by absorbing the wavelength of laser light that will be applied to the tissue. Embodiments of the coating are described in U.S. patent application Ser. No. 12/468,668 filed May 19, 2009 entitled “ADJUVANT ENHANCED ABLATION,” which is incorporated herein by reference in its entirety.

In one embodiment, the balloon 110 is placed in the deflated state 127 and the distal end 108 of the shaft 104 is fed into the cavity of the patent, such as the uterus, where the target tissue is located. In one embodiment, the cavity is visually inspected using the viewing fiber 202.

In one embodiment, the balloon 110 is inflated within the cavity by pumping either fluid or gas through the tubing 250 and the port 140, such as using the pump 144. In one embodiment, the inflated state 128 of the balloon engages the interior wall of the cavity, such as illustrated in FIG. 5.

In one embodiment, the cavity and the inflated balloon 110 are inspected using the viewing fiber 202. This involves moving the distal end 204 of the viewing fiber 202 axially and/or angularly using the one or more viewing fiber positioning components 210.

In one embodiment, the markings 139 on the balloon are imaged or viewed using the viewing fiber 202. The markings indicate whether the balloon 110 is properly inflated and/or positioned within the cavity of the patient. In one embodiment, the balloon 110 is deflated, repositioned and inflated again until the markings 139 indicate that the balloon 110 is fully inflated and/or in the desired position within the cavity.

In one embodiment, the laser fiber 162 is positioned as desired relative to the shaft 104 and the balloon 110 using the one or more laser fiber positioning components 180. This may involve moving the distal end 168 axially, angularly, or along an arc.

In one embodiment, the laser system 160 is activated to transmit laser light 164 through the laser fiber 162 and out the dispenser 166 to ablate the targeted tissue. In one embodiment, this activation of the laser system is responsive to the actuation of the laser actuator 222. In one embodiment, the targeted tissues are inspected using the viewing fiber 202.

In one embodiment, the dispenser 166, the distal end 108 of the shaft 104, and/or the balloon 110 are configured to provide substantially uniform transmission of the laser light 164.

In one embodiment, the dispenser 166, the distal end 108 of the shaft 104, and/or the balloon 110 are configured to provide non-uniform transmission of the laser light to control the exposure of the target tissue to the laser light. In one embodiment, a coating is applied to the shaft 104 and/or the interior of the balloon 110 to control the transmission of the laser light therethrough.

In one embodiment, the distal end 168 of the laser fiber 162 is moved along an arc and/or axially to another position relative to the shaft 104 and the balloon 110 to target other tissue within the cavity of the patient.

In one embodiment, a flow of fluid or gas is circulated through the balloon 110. In one embodiment, the flow of fluid or gas is regulated responsive to a temperature signal from a temperature sensor 212.

Following the completion of the ablation treatment, the balloon 110 is returned to its deflated state 127 and the balloon 110, the shaft 104, the laser fiber 162 and other components of the system (e.g., the viewing fiber 202) are removed from the cavity. The disposable components can then be detached from the laser system 160, the pump 144 and the viewing console 208, removed from the device 102 and discarded.

Although the present invention has been described with reference to preferred embodiments, workers skilled in the art will recognize that changes may be made in form and detail without departing from the spirit and scope of the invention. 

What is claimed is:
 1. An ablation device comprising: a balloon having an open proximal end and a closed distal end; a cylindrical tube extending into the balloon through the proximal end; an end support member engaging an interior side of the distal end of the balloon and a distal end of the cylindrical tube, the end support member extending radially from the cylindrical tube, and radially displacing the balloon from the cylindrical tube; and a seal formed between the proximal end of the balloon and the cylindrical tube.
 2. The device of claim 1, wherein: the end support member is attached to an interior side of the distal end of the balloon comprises a cylindrical portion that faces the proximal end of the balloon and is received within a bore at a distal end of the cylindrical tube and an annular groove surrounding the cylindrical portion; and the distal end of a cylindrical tube is received in the annular groove.
 3. The device of claim 2, wherein: the end support member comprises a recess coaxial to the annular groove; and the device comprises a laser fiber extending through the cylindrical tube, the laser fiber comprising a light dispenser configured to deliver laser light through the tube and the balloon, and a distal end received within the recess of the end support member.
 4. The device of claim 3, wherein: the balloon includes a central axis; and the cylindrical portion, the cylindrical tube and the recess are coaxial to the central axis.
 5. The device of claim 1, wherein the balloon has an inflated shape that is substantially cylindrical.
 6. The device of claim 1, wherein the balloon has an inflated shape that substantially conforms to a cavity select from the group consisting of a uterine cavity, an anal cavity, and esophagus, a trachea, a vagina, a bladder, a urethra and a ureter.
 7. The device of claim 1, wherein the cylindrical tube comprises: first and second openings at the distal end; first and second ports at a proximal end; a first fluid pathway connecting the first port to the first opening; and a second fluid pathway connecting the second port to the second opening.
 8. The device of claim 1, further comprising a central support member within the balloon having a central opening through which the tube extends, the central support member extending radially from the tube, wherein the balloon includes an inflatable portion on a proximal side of the central support member corresponding to the proximal end of the balloon, and an inflatable portion on a distal side of the central support member corresponding to the distal end.
 9. The ablation device of claim 1, wherein: a distal end of the balloon includes an exposed exterior surface; and the cylindrical tube has a longitudinal axis that extends through the exposed exterior surface.
 10. An ablation device comprising: a balloon having an open proximal end, a closed distal end and a central axis; a cylindrical tube extending into the balloon through the proximal end; a central support member within the balloon having a central opening through which the cylindrical tube extends, the central support member extending radially from the cylindrical tube; and a seal formed between the proximal end of the balloon and the cylindrical tube; wherein the balloon includes an inflatable portion on a proximal side of the central support member corresponding to the proximal end, and an inflatable portion on a distal side of the central support member corresponding to the distal end.
 11. The device of claim 10, wherein the central support member supports the cylindrical tube in alignment with the central axis.
 12. The device of claim 11, wherein the central support member displaces a portion of the balloon from the tube.
 13. The device of claim 12, wherein the support member is located along the central axis intermediate the proximal and distal ends of the balloon.
 14. The device of claim 13, wherein the support member is positioned along the central axis closer to the distal end of the balloon than the proximal end of the balloon.
 15. The ablation device of claim 10, wherein: a distal end of the balloon includes an exposed exterior surface; and the cylindrical tube has a longitudinal axis that extends through the exposed exterior surface. 